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A novel mutation, Y103X, and exon skipping in a patient with Hunter disease
G Bonuccelli1, M Filocamo, S Regis
1Laboratorio di Diagnosi Pre e Postnatale di Malattie Metaboliche, Istituto G.Gaslini.
Human Mutation
|March 29, 2000
Abstract
No abstract available in PubMed .
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